All terms in EFO
| Label | Id | Description |
|---|---|---|
| rhabdomyolysis | EFO_0003867 | [Necrosis or disintegration of skeletal muscle often followed by myoglobinuria., A clinical syndrome resulting from direct or indirect muscle injury and subsequent release of myoglobin into the plasma.] |
| MDAMB157 | EFO_0001206 | |
| obsolete_cardiovascular abnormality | EFO_0003848 | [Congenital, inherited, or acquired anomalies of the CARDIOVASCULAR SYSTEM, including the HEART and BLOOD VESSELS.] |
| parasympatholytic | CHEBI_50370 | [A parasympatholytic agent is a substance or activity that reduces the activity of the parasympathetic nervous system.[1] (The parasympathetic nervous system is often colloquially described as the "Feed and Breed" or "Rest and Digest" portion of the autonomic nervous system. The parasympathetic nervous system becomes strongly engaged during or after a meal and during times when the body is at rest.) The term parasympatholytic typically refers to the effect of a drug, although some poisons act to block the parasympathetic nervous system as well. Most drugs with parasympatholytic properties are anticholinergics.] |
| palatal neoplasm | EFO_0003849 | [A benign or malignant neoplasm that affects the hard palate, soft palate, or uvula.] |
| obsolete_Turner syndrome due to structural X chromosome anomalies | Orphanet_99413 | |
| Classical progressive supranuclear palsy | Orphanet_240071 | [Classical progressive supranuclear palsy, also known as Richardson's syndrome, is the most common clinical variant of progressive supranuclear palsy (PSP; see this term), a rare late-onset neurodegenerative disease characterized by postural instability, progressive rigidity, supranuclear gaze palsy and mild dementia.] |
| obsolete_patterned dystrophy of the retinal pigment epithelium | Orphanet_63454 | |
| developmental disability | EFO_0003852 | [Disorders in which there is a delay in development based on that expected for a given age level or stage of development. These impairments or disabilities originate before age 18, may be expected to continue indefinitely, and constitute a substantial impairment. Biological and nonbiological factors are involved in these disorders. (From American Psychiatric Glossary, 6th ed)] |
| intestinal polyp | EFO_0003855 | [Discrete abnormal tissue masses that protrude into the lumen of the intestine. A polyp is attached to the intestinal wall either by a stalk, pedunculus, or by a broad base., Discrete abnormal tissue masses that protrude into the lumen of the INTESTINE. A polyp is attached to the intestinal wall either by a stalk, pedunculus, or by a broad base.] |
| postmenopausal osteoporosis | EFO_0003854 | [Metabolic disorder associated with fractures of the femoral neck, vertebrae, and distal forearm. It occurs commonly in women within 15-20 years after menopause, and is caused by factors associated with menopause including estrogen deficiency.] |
| arthrogryposis | EFO_0003857 | [A rare, non-progressive congenital disorder characterized by multiple joint contractures which are present at birth., Persistent flexure or contracture of a joint. (Dorland, 27th ed)] |
| Secretory diarrhea | HP_0005208 | [Watery voluminous diarrhea resulting from an imbalance between ion and water secretion and absorption.] |
| Met5A | EFO_0001218 | |
| MM1 | EFO_0001219 | |
| multiple myeloma | EFO_0001378 | [A bone marrow-based plasma cell neoplasm characterized by a serum monoclonal protein and skeletal destruction with osteolytic lesions, pathological fractures, bone pain, hypercalcemia, and anemia. Clinical variants include non-secretory myeloma, smoldering myeloma, indolent myeloma, and plasma cell leukemia. (WHO, 2001)] |
| Pancreatic pseudocyst | HP_0005206 | [Cyst-like space not lined by epithelium and contained within the pancreas. Pancreatic pseudocysts are often associated with pancreatitis.] |
| Abnormality of the abdominal organs | HP_0002012 | [An abnormality of the viscera of the abdomen.] |
| dasatinib | CHEBI_49375 | [A N-(2-hydroxyethyl)piperazine that has formula C22H26ClN7O2S., A monounsaturated very long-chain fatty acid with a 22-carbon backbone and a single double bond originating from the 9th position from the methyl end, with the double bond in the trans- configuration.] |
| erythroleukemia cell | BTO_0000426 | [ Cancer cell of the blood-forming tissues in which large numbers of immature, abnormal red blood cells are found in the blood and bone marrow. ] |